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USA - Document Control Specialist I

Cleveland, MS 38732

Posted: 09/15/2023 Employment Type: Contract Job Category: Operations Job Number: 581955 Is job remote?: No Country: United States

Job Description

  • This section focuses on the main purpose of the job in one to four sentences. Review and approve GMP/GLP Manufacturing and related documentation to support timely product and system release. Conduct internal audit of SOPs, training records, and other document types on an as needed basis. Responsible for activities related to providing required documentation and implementing related documentation systems. Participate on project teams as needed. This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned. Review documentation for accuracy and compliance to procedures. Route, release or reject as appropriate. Ensure all document and system elements are identified, accurate and assembled for review and approval.
  • Maintain, proof read, and change as needed Standard Operating Procedures To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
  • Intermediate level and document management (e.g. Word) software skills
  • Project Management Skills
  • Must have excellent conceptual, analytical, written and verbal configuration skills
  • Comprehension of design methodology, product configuration and complex manufacturing processes
  • Ability to work under strict deadlines and changing priorities with minimal supervision
  • Strong interpersonal skills and great attention to detail are necessary
  • Must be a strong team player with good problem solving, and good verbal and written communications skills
  • Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Applications of Good laboratory Practices, and Application of Good Manufacturing Practices Include the education and experience that is necessary to perform the job satisfactorily.
  • B.A. or B.S. and/or 3-5 years related experience (in-house or acquired outside). 
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